A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056988



Internal ID21966224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21551274..21551328hg38UCSC Ensembl
chr19:21734076..21734130hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056988
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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